US5390626A - Process for formation of silicon carbide film - Google Patents

Process for formation of silicon carbide film Download PDF

Info

Publication number
US5390626A
US5390626A US08/037,657 US3765793A US5390626A US 5390626 A US5390626 A US 5390626A US 3765793 A US3765793 A US 3765793A US 5390626 A US5390626 A US 5390626A
Authority
US
United States
Prior art keywords
reactor
source gases
film
flow velocity
substrate
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US08/037,657
Inventor
Hiroyuki Nagasawa
Minoru Sugawara
Kazuhide Yamashiro
Masato Kobayashi
Yohichi Yamaguchi
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Hoya Corp
Original Assignee
Hoya Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Hoya Corp filed Critical Hoya Corp
Priority to US08/037,657 priority Critical patent/US5390626A/en
Application granted granted Critical
Publication of US5390626A publication Critical patent/US5390626A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C30CRYSTAL GROWTH
    • C30BSINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
    • C30B25/00Single-crystal growth by chemical reaction of reactive gases, e.g. chemical vapour-deposition growth
    • C30B25/02Epitaxial-layer growth
    • CCHEMISTRY; METALLURGY
    • C30CRYSTAL GROWTH
    • C30BSINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
    • C30B29/00Single crystals or homogeneous polycrystalline material with defined structure characterised by the material or by their shape
    • C30B29/10Inorganic compounds or compositions
    • C30B29/36Carbides

Definitions

  • the present invention relates to a process for the formation of a silicon carbide (SIC) film to be used as a substrate material for a semiconductor device or as an X-ray transmissive film for an X-ray mask.
  • SIC silicon carbide
  • it relates to a process for the formation of a silicon carbide film by a low pressure CVD method using a hot-wall system.
  • the following systems are available for the formation of an SiC film on a substrate by a CVD method, i.e., a cold-wall system in which a substrate is placed on a susceptor having a surface coated with SiC having a thickness of some hundreds ⁇ m, and an SiC film is formed on the substrate while the substrate is heated by means of thermal conductivity from the inductively heated susceptor, and a hot-wall system in which an SiC film is formed on a substrate while the substrate is indirectly externally heated by heating a reactor (generally made of quartz) with a heater provided on a peripheral surface of the reactor.
  • a reactor generally made of quartz
  • the SiC film formation based on an atmospheric pressure or low pressure CVD method using a cold-wall system is generally carried out by a carbonization method (e.g., Appl. Phys. Lett., Vol. 42, No. 5, pages 480-462 (1985)) or by a two-temperature continuous method (e.g., J. Crys. Growth, Vol. 70, pages 287-290, (1984)). Both these methods involve a rapid increase or a rapid decrease in the temperature of a substrate. However, since the reactor itself has a low temperature, the damage to the reactor due to high temperature during the SiC film formation scarcely occurs. On the other hand, the above methods have the following problems.
  • the uniformity of the SiC film thickness or the SiC film properties on the surface of one substrate or among different substrates is poor as compared with that of film(s) obtained by a CVD method using a hot-wall system. Further, since a substrate is to be placed on a susceptor, the number of substrates that can be treated during one film-forming operation is limited, and the mass productivity is lower than that of a CVD method using a hot-wall system.
  • an SiC film is formed by a conventional atmospheric pressure or low pressure CVD method using a hot-wall system
  • the film formation is carried out while the reactor itself is heated to a temperature equivalent to or higher than the temperature for the formation of the SiC film.
  • the temperature for the formation of an SiC film can be decreased by the use, as one of source gases, of a highly reactive gas such as acetylene (C 2 H 2 ) and dichlorosilane (SiH 2 Cl 2 ).
  • the above object of the present invention is achieved by a process for the formation of a silicon carbide Film which comprises placing at least one substrate in a reactor of a CVD apparatus using a hot-wall system, and introducing a plurality of source gases into the reactor under reduced pressure while the reactor is heated, thereby to form a silicon carbide film on the substrate in the reactor, wherein the source gases comprise at least a dichlorosilane gas and an acetylene gas, the flow velocity of the source gases in the reactor is not less than 70 cm/second, and the temperature for heating the reactor is not more than 1,000° C.
  • the flow velocity of the source gases is influenced by the pressure in the reactor.
  • the pressure in the reactor In order to keep a flow velocity of not less than 70 cm/second in all of the inlet side, the central portion and the exhaust side of the reactor, it is therefore preferable to adjust the pressure in the reactor to not more than 5 Torr.
  • the pressure in the reactor is too low, the growth rate of the SiC film decreases. It is therefore preferable to adjust the pressure to not less than 0.01 Torr in order to attain high mass productivity.
  • the temperature for the formation of the SiC film can be at not more than 1,000° C. Therefore, almost no damage occurs to the reactor by high temperature during the film formation.
  • the flow velocity in the reactor is set at not less than 70 cm/second, the concentration distribution of the source gases in the reactor is rendered uniform. As a result, there can be obtained SiC films which are excellent in the uniformity of the film thickness and film properties on the surface of one substrate and among different substrates.
  • FIG. 1 is a schematic view of a hot-wall type low pressure CVD system used in Example.
  • FIG. 2 is a graph showing the film thickness variability of an SiC film on the surface of one substrate and the film thickness variability of SiC films among substrates when the flow velocity of source gases in a reaction tube was variously changed.
  • FIG. 3 is a graph showing the relationship between the degree of internal stress of each of SiC films obtained by variously changing the flow velocity of source gases in a reaction tube and the position where each of substrates was placed.
  • FIG. 4 is a graph showing the relationship between the composition ratio of each of SiC films obtained by variously changing the flow velocity of source gases in a reaction tube, and the position where each of the substrates was placed.
  • Silicon wafers ((100) face, resistivity 0.5-5.0 ⁇ /cm, N-type) having a diameter of 76 ⁇ 0.5 mm (3 inches) and a thickness of 380 ⁇ 10 ⁇ m were used as a substrate on which an SiC film was to be formed.
  • FIG. 1 shows a resistance heating method-applied hot-wall low pressure CVD system used for the formation of SiC films in this Example.
  • numeral 1 indicates a horizontal reaction tube
  • numeral 2 indicates a resistance heating type heater provided on a peripheral surface of the reaction tube
  • numeral 3 is a quartz-made substrate holder
  • numeral 4 indicates an exhaust pump
  • numeral 5 indicates a butterfly valve
  • numeral 6 indicates a Pirani gauge
  • numeral 9 indicates a mass flow controller.
  • reaction tube 1 was heated with the heater 2, and when the reaction tube 1 was heated, each of the substrates S was also indirectly heated.
  • the temperature in the reaction tube 1 was indirectly measured with a thermocouple (not shown) provided in the vicinity of the heater 2.
  • the flow velocity of the source gases was controlled by changing the pressure in the reaction tube under the adjustment of the butterfly valve 5 provided just before the exhaust pump 4.
  • the source gases introduced into the reaction tube underwent a reaction due to thermal excitation to form an SiC film on each of the substrates S.
  • Table 1 shows the film growth conditions.
  • FIG. 2 shows the variabilities in film thicknesses of SiC films formed at 950° C. on the surface of one substrate and among different substrates.
  • FIG. 2 clearly shows the following.
  • the film thickness variabilities decreased with an increase in the flow velocity of the source gases, and when the flow velocity of the source gases was adjusted to not less than 70 cm/second defined in the present invention, both the film thickness variability on the surface of one substrate and the film thickness variability among substrates were reduced to about 5% or less. That is, when the flow velocity of the source gases was adjusted to not less than 70 cm/second, SiC films having excellent uniformity in film thickness were obtained.
  • FIG. 3 shows the degrees of internal stresses of the SiC films formed at 950° C.
  • FIG. 3 clearly shows the following.
  • the variability (among substrates) of the degrees of internal stresses of the SiC films caused by a positional difference among the substrates in the reaction tube decreased with an increase in the flow velocity of the source gases, and this variability was further decreased by adjusting the flow velocity of the source gases to the range defined in the present invention. That is, SiC films having excellent uniformity of film properties among the substrates were obtained.
  • FIG. 4 shows the composition ratios of the SiC films formed at 950° C.
  • FIG. 4 clearly shows the following.
  • the flow velocity of the source gases was adjusted to the range defined in the present invention, i.e., 117.0 cm/second and 218.0 cm/second even the substrates on the exhaust side had SiC films having a composition ratio of nearly 1. That is, SiC films having uniformity in the film properties among substrates were obtained.
  • the present invention includes the following application embodiments and variations.
  • Example 2 the substrates having a diameter of 3 inches were used for making clear the effects produced by an increase in the flow velocity of the source gases and the effect produced by a decrease in the temperature for forming films, whereas the substrate used in the present invention is not specially limited with regard to the size and form, and there may be used substrates having a diameter or a maximum length of 5 inches or less and having any form.
  • Example 3 SiC films were formed on 33 substrates in one film-forming operation for making clear the effects produced by an increase in the flow velocity of the source gases and the effect produced by a decrease in the temperature for the formation of films, whereas the number of substrates to be placed in the reaction tube for one film-forming operation is not specially limited, and may be properly selected. And these effects can be exhibited regardless of the number of substrates placed in the reaction tube.
  • Example 4 the pressure in the reaction tube was changed by adjusting the butterfly valve so that the flow velocity of the source gases in the reaction tube was adjusted, whereas the flow velocity of the source gases in the reaction tube can be adjusted by controlling the amount of the carrier gas to be introduced per a unit time or the amounts of the source gases to be introduced per a unit time.
  • the present invention permits the production, at a high mass productivity, of SiC films having excellent uniformity in the film thickness and film properties on the surface of one substrate and among different substrates without causing any damage to the reactor from heat during the film formation.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Chemical Vapour Deposition (AREA)

Abstract

In a process for the formation of SiC films by a low pressure CVD method using a hot-wall type, a dichlorosilane gas and an acetylene gas are used as a source gas, the flow velocity of the source gases in a reactor is set at not less than 70 cm/second, and the temperature for heating the reactor is set at not more than 1,000° C., whereby SiC films having excellent uniformity in the film thickness and film properties on the surface of one substrate and among different substrates can be produced at a high mass productivity without causing any damage to the reactor from heat during the film formation.

Description

This is a continuation of application Ser. No. 07/804,992, filed Dec. 10, 1991, now abandoned.
FIELD OF THE INVENTION
The present invention relates to a process for the formation of a silicon carbide (SIC) film to be used as a substrate material for a semiconductor device or as an X-ray transmissive film for an X-ray mask. In particular, it relates to a process for the formation of a silicon carbide film by a low pressure CVD method using a hot-wall system.
PRIOR ART OF THE INVENTION
The following systems are available for the formation of an SiC film on a substrate by a CVD method, i.e., a cold-wall system in which a substrate is placed on a susceptor having a surface coated with SiC having a thickness of some hundreds μm, and an SiC film is formed on the substrate while the substrate is heated by means of thermal conductivity from the inductively heated susceptor, and a hot-wall system in which an SiC film is formed on a substrate while the substrate is indirectly externally heated by heating a reactor (generally made of quartz) with a heater provided on a peripheral surface of the reactor. When the pressure used for these two systems, atmospheric pressure or reduced pressure, is taken into consideration, there are four film-forming methods.
Since, however, the temperature for the formation of an SiC film is generally 1,300° C. or higher, it is necessary to prevent a damage to a reactor. Therefore, an atmospheric pressure or low pressure CVD method using a cold-wall system is applied to a process for the formation of an SiC film by a CVD method.
The SiC film formation based on an atmospheric pressure or low pressure CVD method using a cold-wall system is generally carried out by a carbonization method (e.g., Appl. Phys. Lett., Vol. 42, No. 5, pages 480-462 (1985)) or by a two-temperature continuous method (e.g., J. Crys. Growth, Vol. 70, pages 287-290, (1984)). Both these methods involve a rapid increase or a rapid decrease in the temperature of a substrate. However, since the reactor itself has a low temperature, the damage to the reactor due to high temperature during the SiC film formation scarcely occurs. On the other hand, the above methods have the following problems. Since substrate(s) is(are) heated through susceptor(s), the uniformity of the SiC film thickness or the SiC film properties on the surface of one substrate or among different substrates is poor as compared with that of film(s) obtained by a CVD method using a hot-wall system. Further, since a substrate is to be placed on a susceptor, the number of substrates that can be treated during one film-forming operation is limited, and the mass productivity is lower than that of a CVD method using a hot-wall system.
It is therefore desired to apply an atmospheric pressure or low pressure CVD method using a hot-wall system to the production, at a high mass productivity, of SiC films which are so excellent in the film thickness uniformity that the film thickness variability on the surface of one substrate or among different substrates is, for example, about 5 % or less and which are also excellent in the film properties on the surface of one substrate or among different substrates.
However, when an SiC film is formed by a conventional atmospheric pressure or low pressure CVD method using a hot-wall system, the film formation is carried out while the reactor itself is heated to a temperature equivalent to or higher than the temperature for the formation of the SiC film. There is therefore a problem in that the reactor is damaged due to high temperature during the film formation as described above. The temperature for the formation of an SiC film can be decreased by the use, as one of source gases, of a highly reactive gas such as acetylene (C2 H2) and dichlorosilane (SiH2 Cl2). However, the problem with the use of such a highly reactive gas in a conventional CVD method using a hot-wall system is that since the source gas concentration distribution in the reactor is rendered nonuniform, no SiC film having excellent uniformity in the film thickness and film properties can be obtained.
It is therefore an object of the present invention to provide a process for the formation of an SiC film, which permits the production, at a high mass productivity, of an SiC film which is excellent in uniformity of the film thickness and film properties on the surface of one substrate and among different substrates without causing any damage to the reactor from heat during the film formation.
SUMMARY OF THE INVENTION
The above object of the present invention is achieved by a process for the formation of a silicon carbide Film which comprises placing at least one substrate in a reactor of a CVD apparatus using a hot-wall system, and introducing a plurality of source gases into the reactor under reduced pressure while the reactor is heated, thereby to form a silicon carbide film on the substrate in the reactor, wherein the source gases comprise at least a dichlorosilane gas and an acetylene gas, the flow velocity of the source gases in the reactor is not less than 70 cm/second, and the temperature for heating the reactor is not more than 1,000° C.
In the above process, the flow velocity of the source gases is influenced by the pressure in the reactor. In order to keep a flow velocity of not less than 70 cm/second in all of the inlet side, the central portion and the exhaust side of the reactor, it is therefore preferable to adjust the pressure in the reactor to not more than 5 Torr. However, when the pressure in the reactor is too low, the growth rate of the SiC film decreases. It is therefore preferable to adjust the pressure to not less than 0.01 Torr in order to attain high mass productivity.
In the process of the present invention for the formation of an SiC film by a hot-wall low pressure CVD system using a dichlorosilane gas and an acetylene gas, the temperature for the formation of the SiC film can be at not more than 1,000° C. Therefore, almost no damage occurs to the reactor by high temperature during the film formation.
Further, due to the use of the above source gases, a sufficiently high film growth rate can be maintained even at a film growth temperature of not more than 1,000° C. Moreover, due to the hot-wall system, the number of substrates treated in one film-forming operation is large. That is, the process of the present invention is excellent in mass productivity.
Further, since the flow velocity in the reactor is set at not less than 70 cm/second, the concentration distribution of the source gases in the reactor is rendered uniform. As a result, there can be obtained SiC films which are excellent in the uniformity of the film thickness and film properties on the surface of one substrate and among different substrates.
BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 is a schematic view of a hot-wall type low pressure CVD system used in Example.
FIG. 2 is a graph showing the film thickness variability of an SiC film on the surface of one substrate and the film thickness variability of SiC films among substrates when the flow velocity of source gases in a reaction tube was variously changed.
FIG. 3 is a graph showing the relationship between the degree of internal stress of each of SiC films obtained by variously changing the flow velocity of source gases in a reaction tube and the position where each of substrates was placed.
FIG. 4 is a graph showing the relationship between the composition ratio of each of SiC films obtained by variously changing the flow velocity of source gases in a reaction tube, and the position where each of the substrates was placed.
The present invention will be detailed hereinafter by reference to Example and Comparative Example.
EXAMPLE AND COMPARATIVE EXAMPLE
Silicon wafers ((100) face, resistivity 0.5-5.0 Ω/cm, N-type) having a diameter of 76±0.5 mm (3 inches) and a thickness of 380±10 μm were used as a substrate on which an SiC film was to be formed. A dichlorosilane gas (SiH2 Cl2) and an acetylene gas (C2 H2) were used as a source gas, and a hydrogen gas (H2) was used as a carrier gas.
FIG. 1 shows a resistance heating method-applied hot-wall low pressure CVD system used for the formation of SiC films in this Example. In FIG. 1, numeral 1 indicates a horizontal reaction tube, numeral 2 indicates a resistance heating type heater provided on a peripheral surface of the reaction tube 1, numeral 3 is a quartz-made substrate holder, numeral 4 indicates an exhaust pump, numeral 5 indicates a butterfly valve, numeral 6 indicates a Pirani gauge, and numeral 9 indicates a mass flow controller.
As shown in FIG. 1, thirty-three substrates S were vertically placed on the substrate holder S at intervals of 5 mm, and the pressure in the reaction tube 1 was reduced to a vacuum of 1.0×10-3 Torr by actuating the exhaust valve 4. Then, SiH2 Cl2, C2 H2 and H2 were introduced into the reaction tube 1 at a predetermined flow velocity. In this case, the flow velocity of the source gases in the reaction tube was variously changed by changing the pressure in the reaction tube, whereby SiC films were formed on the substrates S. The temperature in the reaction tube (corresponding to a film growth temperature) was varied in the range between 800° C. and 1,000° C.
In addition, the reaction tube 1 was heated with the heater 2, and when the reaction tube 1 was heated, each of the substrates S was also indirectly heated. The temperature in the reaction tube 1 was indirectly measured with a thermocouple (not shown) provided in the vicinity of the heater 2. The flow velocity of the source gases was controlled by changing the pressure in the reaction tube under the adjustment of the butterfly valve 5 provided just before the exhaust pump 4. The source gases introduced into the reaction tube underwent a reaction due to thermal excitation to form an SiC film on each of the substrates S.
Table 1 shows the film growth conditions.
              TABLE 1                                                     
______________________________________                                    
Substrate           Si (100) wafer                                        
Growth temperature  800-1,000°                                     
                             C.                                           
Flow amounts                                                              
of source gases                                                           
SiH.sub.2 Cl.sub.2  200      sccm                                         
C.sub.2 H.sub.2     30       sccm                                         
Flow velocity of source gases                                             
                    11.4-230 cm/second                                    
Pressure in reaction tube                                                 
                    0.10-10  Torr                                         
______________________________________                                    
Each of the SiC films obtained by changing the film growth conditions as above was measured for a thickness on the basis of reflection spectrum of visible light beam. The film thickness variability on the surface of one substrate and the variability among substrates were expressed by percentages of 3δn-1 (n≧17) to an average of the measured film thickness values, and the films were evaluated on uniformity of film thickness according to the percentages. FIG. 2 shows the variabilities in film thicknesses of SiC films formed at 950° C. on the surface of one substrate and among different substrates.
FIG. 2 clearly shows the following. The film thickness variabilities decreased with an increase in the flow velocity of the source gases, and when the flow velocity of the source gases was adjusted to not less than 70 cm/second defined in the present invention, both the film thickness variability on the surface of one substrate and the film thickness variability among substrates were reduced to about 5% or less. That is, when the flow velocity of the source gases was adjusted to not less than 70 cm/second, SiC films having excellent uniformity in film thickness were obtained.
Further, as one method of evaluation, among substrates, of the properties of SiC films obtained by variously changing the film growth conditions, the degrees of internal stresses in the SiC films were compared. FIG. 3 shows the degrees of internal stresses of the SiC films formed at 950° C.
FIG. 3 clearly shows the following. The variability (among substrates) of the degrees of internal stresses of the SiC films caused by a positional difference among the substrates in the reaction tube decreased with an increase in the flow velocity of the source gases, and this variability was further decreased by adjusting the flow velocity of the source gases to the range defined in the present invention. That is, SiC films having excellent uniformity of film properties among the substrates were obtained.
Further, as another method of evaluation, among substrates, of the properties of SiC films obtained by variously changing the film growth conditions, composition ratios of the SiC films were compared. FIG. 4 shows the composition ratios of the SiC films formed at 950° C.
FIG. 4 clearly shows the following. The tendency to vary in the composition ratio of the SiC film, caused by a positional difference among the substrates in the reaction tube, i.e., the tendency of the substrates near the exhaust side toward formation of Si-richer SiC films, decreased with an increase in the flow velocity of the source gases. When the flow velocity of the source gases was adjusted to the range defined in the present invention, i.e., 117.0 cm/second and 218.0 cm/second even the substrates on the exhaust side had SiC films having a composition ratio of nearly 1. That is, SiC films having uniformity in the film properties among substrates were obtained.
In addition, no damage to the reaction tube by heat during the film formation was recognized under any of the film growth conditions.
In addition to the above Example, the present invention includes the following application embodiments and variations.
1) In addition to silicon wafers used in Examples, there may be used other substrates of glass, SIC, and the like.
2) In Example, the substrates having a diameter of 3 inches were used for making clear the effects produced by an increase in the flow velocity of the source gases and the effect produced by a decrease in the temperature for forming films, whereas the substrate used in the present invention is not specially limited with regard to the size and form, and there may be used substrates having a diameter or a maximum length of 5 inches or less and having any form.
3) In Example, SiC films were formed on 33 substrates in one film-forming operation for making clear the effects produced by an increase in the flow velocity of the source gases and the effect produced by a decrease in the temperature for the formation of films, whereas the number of substrates to be placed in the reaction tube for one film-forming operation is not specially limited, and may be properly selected. And these effects can be exhibited regardless of the number of substrates placed in the reaction tube.
4) In Example, the pressure in the reaction tube was changed by adjusting the butterfly valve so that the flow velocity of the source gases in the reaction tube was adjusted, whereas the flow velocity of the source gases in the reaction tube can be adjusted by controlling the amount of the carrier gas to be introduced per a unit time or the amounts of the source gases to be introduced per a unit time.
As specified above, the present invention permits the production, at a high mass productivity, of SiC films having excellent uniformity in the film thickness and film properties on the surface of one substrate and among different substrates without causing any damage to the reactor from heat during the film formation.

Claims (10)

What is claimed is:
1. A process for the formation of a silicon carbide film which comprises placing at least one substrate in a reactor of a CVD system using a hot-wall, and introducing a plurality of source gases into the reactor under reduced pressure while the reactor is heated, thereby to form a silicon carbide film in which the composition ratio of Si to C is about 1 on the substrate in the reactor, wherein the source gases comprise at least a dichlorosilane gas and an acetylene gas, the flow velocity of the source gases in the reactor is at least 70 cm/second, and the temperature for heating the reactor is not more than 1,000° C.
2. A process according to claim 1, wherein the reactor is adjusted to a pressure between 0.01 Torr and 5 Torr.
3. A process according to claim 1, wherein the substrate is selected from the group consisting of a silicon wafer, glass and SiC.
4. A process according to claim 1, wherein a carrier gas is introduced into the reactor together with the source gases.
5. A process according to claim 4, wherein the carrier gas is a hydrogen gas.
6. A process according to claim 1, wherein the temperature for heating is between 800° C. and 1,000° C.
7. A process according to claim 1, wherein the flow velocity of the source gases in the reactor is adjusted by changing a pressure in the reactor.
8. A process according to claim 1, wherein the flow velocity of the source gases in the reactor is adjusted by controlling an amount of a carrier gas to be introduced per a unit time.
9. A process according to claim 1, wherein the flow velocity of the source gases in the reactor is adjusted by controlling an amount of the source gases to be introduced per a unit time.
10. An X-ray transmissive film containing a silicon carbide film obtained by the process recited in claim 1.
US08/037,657 1990-12-11 1993-03-26 Process for formation of silicon carbide film Expired - Lifetime US5390626A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US08/037,657 US5390626A (en) 1990-12-11 1993-03-26 Process for formation of silicon carbide film

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
JP2401435A JP2556621B2 (en) 1990-12-11 1990-12-11 Method for forming silicon carbide film
JP2-0401435 1990-12-11
US80499291A 1991-12-10 1991-12-10
US08/037,657 US5390626A (en) 1990-12-11 1993-03-26 Process for formation of silicon carbide film

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
US80499291A Continuation 1990-12-11 1991-12-10

Publications (1)

Publication Number Publication Date
US5390626A true US5390626A (en) 1995-02-21

Family

ID=18511262

Family Applications (1)

Application Number Title Priority Date Filing Date
US08/037,657 Expired - Lifetime US5390626A (en) 1990-12-11 1993-03-26 Process for formation of silicon carbide film

Country Status (2)

Country Link
US (1) US5390626A (en)
JP (1) JP2556621B2 (en)

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5487358A (en) * 1992-12-09 1996-01-30 Shin-Etsu Handotai Co., Ltd. Apparatus for growing silicon epitaxial layer
US5670414A (en) * 1996-02-06 1997-09-23 National Science Council Graded-gap process for growing a SiC/Si heterojunction structure
US5707451A (en) * 1994-02-03 1998-01-13 Applied Materials, Inc. Method and apparatus for cleaning a throttle valve
US5906680A (en) * 1986-09-12 1999-05-25 International Business Machines Corporation Method and apparatus for low temperature, low pressure chemical vapor deposition of epitaxial silicon layers
US20030045102A1 (en) * 2001-08-27 2003-03-06 Hoya Corporation Method of manufacturing compound single crystal
US20030056718A1 (en) * 2001-09-27 2003-03-27 Hoya Corporation Method of manufacturing single crystal substrate
US6736894B2 (en) 2001-08-27 2004-05-18 Hoya Corporation Method of manufacturing compound single crystal
US6821340B2 (en) * 2000-05-31 2004-11-23 Hoya Corporation Method of manufacturing silicon carbide, silicon carbide, composite material, and semiconductor element
US20060288933A1 (en) * 2005-06-27 2006-12-28 Arima Computer Corporation Chemical vapor deposition reactor
US20070169687A1 (en) * 2006-01-26 2007-07-26 Caracal, Inc. Silicon carbide formation by alternating pulses
US7261919B2 (en) * 2003-11-18 2007-08-28 Flx Micro, Inc. Silicon carbide and other films and method of deposition
US20100276702A1 (en) * 2007-05-31 2010-11-04 Chien-Min Sung Doped Diamond LED Devices and Associated Methods
US8157914B1 (en) 2007-02-07 2012-04-17 Chien-Min Sung Substrate surface modifications for compositional gradation of crystalline materials and associated products
JP2015510691A (en) * 2012-01-30 2015-04-09 クラッシック ダブリュビージー セミコンダクターズ エービーClassic WBG Semiconductors AB Silicon carbide crystal growth in a CVD reactor using a chlorination chemistry system.

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000297375A (en) * 1999-04-09 2000-10-24 Hoya Corp Production of silicon carbide film, producing device therefor and production of x-ray mask
JP3915697B2 (en) * 2002-01-15 2007-05-16 東京エレクトロン株式会社 Film forming method and film forming apparatus
JP5564311B2 (en) * 2009-05-19 2014-07-30 株式会社日立国際電気 Semiconductor device manufacturing method, substrate processing apparatus, and substrate manufacturing method

Citations (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3865647A (en) * 1970-09-30 1975-02-11 Siemens Ag Method for precipitation of semiconductor material
JPS61199627A (en) * 1985-02-28 1986-09-04 Oki Electric Ind Co Ltd Manufacture of amorphous multilayer thin film
US4623425A (en) * 1983-04-28 1986-11-18 Sharp Kabushiki Kaisha Method of fabricating single-crystal substrates of silicon carbide
JPH01262500A (en) * 1988-04-13 1989-10-19 Hitachi Ltd X-ray transmittable film
US4897149A (en) * 1985-06-19 1990-01-30 Sharp Kabushiki Kaisha Method of fabricating single-crystal substrates of silicon carbide
US4912063A (en) * 1987-10-26 1990-03-27 North Carolina State University Growth of beta-sic thin films and semiconductor devices fabricated thereon
JPH02157196A (en) * 1988-12-08 1990-06-15 Nec Corp Method for growing semiconductor crystal
JPH02262324A (en) * 1989-03-31 1990-10-25 Hoya Corp X-ray transmitting film and its manufacture
US5001380A (en) * 1987-06-05 1991-03-19 Popov Nikolai P Rotor for an asynchronous motor with multiple layered screen
US5005075A (en) * 1989-01-31 1991-04-02 Hoya Corporation X-ray mask and method of manufacturing an X-ray mask
US5011549A (en) * 1987-10-26 1991-04-30 North Carolina State University Homoepitaxial growth of Alpha-SiC thin films and semiconductor devices fabricated thereon

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5832412A (en) * 1981-08-20 1983-02-25 Sumitomo Electric Ind Ltd Vapor growth apparatus

Patent Citations (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3865647A (en) * 1970-09-30 1975-02-11 Siemens Ag Method for precipitation of semiconductor material
US4623425A (en) * 1983-04-28 1986-11-18 Sharp Kabushiki Kaisha Method of fabricating single-crystal substrates of silicon carbide
JPS61199627A (en) * 1985-02-28 1986-09-04 Oki Electric Ind Co Ltd Manufacture of amorphous multilayer thin film
US4897149A (en) * 1985-06-19 1990-01-30 Sharp Kabushiki Kaisha Method of fabricating single-crystal substrates of silicon carbide
US5001380A (en) * 1987-06-05 1991-03-19 Popov Nikolai P Rotor for an asynchronous motor with multiple layered screen
US4912063A (en) * 1987-10-26 1990-03-27 North Carolina State University Growth of beta-sic thin films and semiconductor devices fabricated thereon
US5011549A (en) * 1987-10-26 1991-04-30 North Carolina State University Homoepitaxial growth of Alpha-SiC thin films and semiconductor devices fabricated thereon
JPH01262500A (en) * 1988-04-13 1989-10-19 Hitachi Ltd X-ray transmittable film
JPH02157196A (en) * 1988-12-08 1990-06-15 Nec Corp Method for growing semiconductor crystal
US5005075A (en) * 1989-01-31 1991-04-02 Hoya Corporation X-ray mask and method of manufacturing an X-ray mask
JPH02262324A (en) * 1989-03-31 1990-10-25 Hoya Corp X-ray transmitting film and its manufacture

Cited By (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5906680A (en) * 1986-09-12 1999-05-25 International Business Machines Corporation Method and apparatus for low temperature, low pressure chemical vapor deposition of epitaxial silicon layers
US5487358A (en) * 1992-12-09 1996-01-30 Shin-Etsu Handotai Co., Ltd. Apparatus for growing silicon epitaxial layer
US5707451A (en) * 1994-02-03 1998-01-13 Applied Materials, Inc. Method and apparatus for cleaning a throttle valve
US5670414A (en) * 1996-02-06 1997-09-23 National Science Council Graded-gap process for growing a SiC/Si heterojunction structure
US6821340B2 (en) * 2000-05-31 2004-11-23 Hoya Corporation Method of manufacturing silicon carbide, silicon carbide, composite material, and semiconductor element
US20030045102A1 (en) * 2001-08-27 2003-03-06 Hoya Corporation Method of manufacturing compound single crystal
US6736894B2 (en) 2001-08-27 2004-05-18 Hoya Corporation Method of manufacturing compound single crystal
US20030056718A1 (en) * 2001-09-27 2003-03-27 Hoya Corporation Method of manufacturing single crystal substrate
US20110001143A1 (en) * 2003-11-18 2011-01-06 Flx Micro, Inc. Composition Comprising Silicon Carbide
US7261919B2 (en) * 2003-11-18 2007-08-28 Flx Micro, Inc. Silicon carbide and other films and method of deposition
USRE42887E1 (en) * 2003-11-18 2011-11-01 Case Western Reserve University Silicon carbide and other films and method of deposition
US8153280B2 (en) 2003-11-18 2012-04-10 Case Western Reserve University Composition comprising silicon carbide
US20060288933A1 (en) * 2005-06-27 2006-12-28 Arima Computer Corporation Chemical vapor deposition reactor
US20070169687A1 (en) * 2006-01-26 2007-07-26 Caracal, Inc. Silicon carbide formation by alternating pulses
US8157914B1 (en) 2007-02-07 2012-04-17 Chien-Min Sung Substrate surface modifications for compositional gradation of crystalline materials and associated products
US8506707B1 (en) 2007-02-07 2013-08-13 Chien-Min Sung Substrate surface modifications for compositional gradation of crystalline materials and associated products
US20100276702A1 (en) * 2007-05-31 2010-11-04 Chien-Min Sung Doped Diamond LED Devices and Associated Methods
US8008668B2 (en) 2007-05-31 2011-08-30 Chien-Min Sung Doped diamond LED devices and associated methods
JP2015510691A (en) * 2012-01-30 2015-04-09 クラッシック ダブリュビージー セミコンダクターズ エービーClassic WBG Semiconductors AB Silicon carbide crystal growth in a CVD reactor using a chlorination chemistry system.

Also Published As

Publication number Publication date
JPH04210476A (en) 1992-07-31
JP2556621B2 (en) 1996-11-20

Similar Documents

Publication Publication Date Title
US5390626A (en) Process for formation of silicon carbide film
US5876797A (en) Low temperature high pressure silicon deposition method
US5874129A (en) Low temperature, high pressure silicon deposition method
US5254370A (en) Method for forming a silicon carbide film
JP3581388B2 (en) Deposited polysilicon film with improved uniformity and apparatus therefor
EP0704551B1 (en) Method of processing a substrate in a vacuum processing chamber
US5932286A (en) Deposition of silicon nitride thin films
US5695819A (en) Method of enhancing step coverage of polysilicon deposits
US4504521A (en) LPCVD Deposition of tantalum silicide
US20010041218A1 (en) High rate silicon nitride deposition method at low pressures
US6287635B1 (en) High rate silicon deposition method at low pressures
US5510297A (en) Process for uniform deposition of tungsten silicide on semiconductor wafers by treatment of susceptor having aluminum nitride surface thereon with tungsten silicide after cleaning of susceptor
US5750195A (en) Deposition of diamond on oxidizable material
US20050013937A1 (en) Thermal gradient enhanced CVD deposition at low pressure
EP1123423B1 (en) High rate silicon deposition method at low pressures
JP3788836B2 (en) Vapor growth susceptor and manufacturing method thereof
US5232868A (en) Method for forming a thin semiconductor film
KR20050107510A (en) Epitaxial semiconductor deposition methods and structrures
JPS6010108B2 (en) Method for pyrolytically depositing silicon nitride onto a substrate
JP2762576B2 (en) Vapor phase growth equipment
KR940010158B1 (en) Tungsten film depositing method using pecvd
WO2000016387A1 (en) High rate silicon nitride deposition method at low pressures
JPH02138726A (en) Manufacture of compound semiconductor device
WO1989005872A1 (en) Vacuum deposition process
JPH0580137B2 (en)

Legal Events

Date Code Title Description
STPP Information on status: patent application and granting procedure in general

Free format text: APPLICATION UNDERGOING PREEXAM PROCESSING

FPAY Fee payment

Year of fee payment: 4

FPAY Fee payment

Year of fee payment: 8

FEPP Fee payment procedure

Free format text: PAYOR NUMBER ASSIGNED (ORIGINAL EVENT CODE: ASPN); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY

FPAY Fee payment

Year of fee payment: 12